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CAS

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207612-71-3

1-(4'-Bromo-biphenyl-4-yl)-naphthalene is a chemical compound characterized by a naphthalene core with a 1-(4'-Bromo-biphenyl-4-yl) group attached to it. It is recognized for its aromatic properties and is frequently utilized in research and development, particularly within the realms of organic synthesis and materials science.

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  • 207612-71-3 Structure

  • Basic information

    1. Product Name: 1-(4'-Bromo-biphenyl-4-yl)-naphthalene
    2. Synonyms: 1-(4'-Bromo-biphenyl-4-yl)-naphthalene
    3. CAS NO:207612-71-3
    4. Molecular Formula:
    5. Molecular Weight: 359.265
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 207612-71-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(4'-Bromo-biphenyl-4-yl)-naphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4'-Bromo-biphenyl-4-yl)-naphthalene(207612-71-3)
    11. EPA Substance Registry System: 1-(4'-Bromo-biphenyl-4-yl)-naphthalene(207612-71-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 207612-71-3(Hazardous Substances Data)

207612-71-3 Usage

Uses

Used in Research and Development:
1-(4'-Bromo-biphenyl-4-yl)-naphthalene is used as a research compound for its potential applications in organic synthesis and materials science. Its unique structure allows for further exploration and development of new compounds and materials with enhanced properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(4'-Bromo-biphenyl-4-yl)-naphthalene is used as a precursor for the synthesis of other compounds. Its chemical structure makes it a promising candidate for the development of new drugs, potentially leading to novel therapeutic agents.
Used in Chemical Synthesis:
1-(4'-Bromo-biphenyl-4-yl)-naphthalene is employed as a key intermediate in chemical synthesis, particularly for creating complex organic molecules. Its unique structure and reactivity contribute to the development of new chemical entities with specific applications in various industries.
Used in Materials Science:
Within the field of materials science, 1-(4'-Bromo-biphenyl-4-yl)-naphthalene is used as a component in the development of advanced materials. Its aromatic properties and structural characteristics can be leveraged to create materials with improved performance, such as enhanced stability, conductivity, or optical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 207612-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,1 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 207612-71:
(8*2)+(7*0)+(6*7)+(5*6)+(4*1)+(3*2)+(2*7)+(1*1)=113
113 % 10 = 3
So 207612-71-3 is a valid CAS Registry Number.

207612-71-3Downstream Products

207612-71-3Relevant articles and documents

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE

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, (2021/08/20)

Provided is an organic electroluminescent element comprising a compound that is represented by formula (1) and having a more improved lifetime. (In the formula, X, R1-R8, R11-R17, R21-R30, L1, L2, n, and Ar1-Ar3 are as defined in the description.)

Compound for capping layer and organic light-emitting device comprising same

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Paragraph 0178-0181, (2020/12/10)

The present invention relates to a compound for a capping layer and an organic light-emitting device comprising the same, the compound for a capping layer according to one embodiment of the present invention being suitable for an organic light-emitting device and being capable of improving the external light-emitting efficiency, chromaticity coordinates, and lifespan of the organic light-emittingdevice.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE SAME

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Page/Page column 48, (2011/08/07)

Disclosed is a long-life organic EL device having high luminous efficiency even after storage at high temperatures. Also disclosed is an aromatic amine derivative which enables to realize such an organic EL device. The aromatic amine derivative is represented by the following general formula (1). (In the formula (1), Ar1 is represented by the general formula (2) below, and Ar2 is represented by the general formula (3) below.)

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

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Page/Page column 68, (2008/06/13)

Disclosed is an organic electroluminescent device wherein an organic thin film which is composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains a novel aromatic amine derivative, which has an asymmetric structure wherein two different amine units are bonded through a linking group, by itself or as a component of a mixture, molecules are hardly crystallized, thereby improving the production yield of the organic electroluminescent device. This organic electroluminescent device has a long life.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

-

Page/Page column 65, (2008/06/13)

Disclosed is a novel aromatic amine derivative having an asymmetric structure. Also disclosed is an organic electroluminescent device wherein an organic thin film composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode. Since at least one layer of the organic thin film contains the aromatic amine derivative by itself or as a component of a mixture, molecules are hardly crystallized, thereby improving the production yield of the organic electroluminescent device. This organic electroluminescent device has a long life.

Suzuki Coupling of Chiral 1,1′-Binaphthyl Systems - New Synthetic Routes to Functionalize the 2- and 2,2′-Positions

Schilling, Birgit,Kaufmann, Dieter E.

, p. 701 - 709 (2007/10/03)

1,1′-Binaphthyl derivatives 1-5, substituted in the 2- or 2,2′-positions are used in palladium-catalyzed Suzuki coupling reactions. The mono- and bis-borylated coupling components 2, 4 and 5 can easily be prepared and purified, are air-stable and are therefore interesting starting materials for Suzuki coupling reactions with several aryl halides. Thus a variety of new axially-chiral 2- and 2,2′-arylated 1,1′-binaphthyls can be synthesized. Selective monoarylation of 3, 4 and 5 can be performed. Subsequent and stepwise arylation offers general access to unsymmetrically substituted binaphthyls. Moreover, interesting atropisomeric complex molecules, such as 4,4′-bis[2-(1,1′-binaphthyl)]-1,1′-biphenyl (18a), are accessible. Compounds of type 18, which can be obtained by twofold Pd-catalyzed coupling reactions, are of high potential value as ligands or promoters in catalytic, asymmetric processes or as chiral precursor molecules for host-guest interactions.

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